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Indoline

CAS No.
496-15-1
Chemical Name:
Indoline
Synonyms
Dihydroindole;2,3-DIHYDRO-1H-INDOLE;2,3-DIHYDROINDOLE;1H-Indole, 2,3-dihydro-;IDN;NDOLINE;INDOLINE;1-Azaindan;1H-Indoline;Indoline>
CBNumber:
CB5485525
Molecular Formula:
C8H9N
Molecular Weight:
119.16
MDL Number:
MFCD00005705
MOL File:
496-15-1.mol
MSDS File:
SDS
Last updated:2023-10-21 16:11:00

Indoline Properties

Melting point -21 °C
Boiling point 220-221 °C (lit.)
Density 1.063 g/mL at 25 °C (lit.)
refractive index n20/D 1.592(lit.)
Flash point 199 °F
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility 5g/l
pka 5.20±0.20(Predicted)
form liquid (clear)
color clear dark brown
Water Solubility 5 g/L (20 ºC)
Sensitive Light Sensitive
BRN 111915
CAS DataBase Reference 496-15-1(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII 6DPT9AB2NK
NIST Chemistry Reference 1H-Indole, 2,3-dihydro-(496-15-1)
EPA Substance Registry System 1H-Indole, 2,3-dihydro- (496-15-1)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H227-H302-H315-H319-H335
Precautionary statements  P210e-P261-P280a-P305+P351+P338-P405-P501a
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  23-24/25-37/39-26
WGK Germany  3
RTECS  NL6906300
Hazard Note  Irritant
TSCA  Yes
HS Code  29339990
NFPA 704
2
1 0

Indoline price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich I5605 Indoline ReagentPlus , 99% 496-15-1 25g $40.9 2024-03-01 Buy
Sigma-Aldrich I5605 Indoline ReagentPlus , 99% 496-15-1 100g $71.4 2024-03-01 Buy
TCI Chemical I0033 Indoline >98.0%(GC)(T) 496-15-1 25mL $34 2024-03-01 Buy
TCI Chemical I0033 Indoline >98.0%(GC)(T) 496-15-1 250mL $191 2024-03-01 Buy
Alfa Aesar A11000 Indoline, 99% 496-15-1 50g $61.7 2024-03-01 Buy
Product number Packaging Price Buy
I5605 25g $40.9 Buy
I5605 100g $71.4 Buy
I0033 25mL $34 Buy
I0033 250mL $191 Buy
A11000 50g $61.7 Buy

Indoline Chemical Properties,Uses,Production

Chemical Properties

?2,3-Dihydroindole [496-15-1], indoline C8H9N, Mr 119.16, bp 229 – 230 ℃(101.3 kPa), is a colorless liquid, which is volatile in steam and soluble in diethyl ether, acetone, and benzene, but only slightly soluble in water. Indoline is obtained by hydrogenation of indole or by catalytic cyclodehydration of 2-(2-aminophenyl)ethanol. A range of pharmaceuticals, as well as fungicides and bactericides, can be produced from indoline.

Uses

As an indole derivative, Indoline can be used in the preparation of various medicinal compounds such as potential α1-adrenoceptor (α1-AR) antagonists.

Uses

Indole is used in perfumery and in preparing tryptophan, one of the 20 amino acids commonly found in animal proteins. It has important application in the industry of plant growth. It is used to prepare indoleacetic acid (auxin) and other plant growth substances which help the development of roots in plant. Indole and its derivatives are widely used in making perfumes, dyes, agrochemicals and medicines.

Uses

Reactant for preparation of:

  • Inhibitors of NOD1-Induced Nuclear Factor-κB Activation
  • Sphingosine-1-phosphate 4(S1P4) receptor antagonists
  • Cytotoxic cell cycle inhibitors
  • 2-Aminopyridines
  • PET agent for imaging of protein kinase C (PKC)
  • Sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors for the management of hyperglycemia in diabetes
  • α4β2-Nicotinic acetylcholine receptor-selective partial agonists
  • mGlu4 positive allosteric modulators
  • Bacterial biofilm inhibitors
  • Serotonin 5-HT6 receptor antagonists

Definition

ChEBI: Indoline is a member of indoles.

Synthesis Reference(s)

Journal of the American Chemical Society, 96, p. 7812, 1974 DOI: 10.1021/ja00832a035
Synthetic Communications, 13, p. 489, 1983 DOI: 10.1080/00397918308081827

120-72-9
496-15-1
Synthesis of Indoline from Indole
Global( 473)Suppliers
Supplier Tel Email Country ProdList Advantage
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 47465 58
Hangzhou Verychem Science And Technology Co.Ltd
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Hebei Mojin Biotechnology Co., Ltd
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Henan Fengda Chemical Co., Ltd
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Capot Chemical Co.,Ltd.
571-85586718 +8613336195806 sales@capotchem.com China 29797 60
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Henan Tianfu Chemical Co.,Ltd.
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Shanghai Time Chemicals CO., Ltd.
+86-021-57951555 +8617317452075 jack.li@time-chemicals.com China 1807 55
Hangzhou FandaChem Co.,Ltd.
008657128800458; +8615858145714 fandachem@gmail.com China 9350 55
AB PharmaTech,LLC
323-480-4688 United States 989 55

View Lastest Price from Indoline manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Indoline pictures 2024-04-23 Indoline
496-15-1
US $5.00 / kg 1kg ≥99% 500mt/year Jinan Finer Chemical Co., Ltd
Indoline pictures 2024-01-02 Indoline
496-15-1
US $200.00-1.00 / KG 1KG 99%, 99.5% Sublimated g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Indoline pictures 2023-11-01 Indoline
496-15-1
US $0.00-0.00 / kg 0.1kg 99.0%min 200kg Hangzhou ICH Biofarm Co., Ltd
  • Indoline pictures
  • Indoline
    496-15-1
  • US $5.00 / kg
  • ≥99%
  • Jinan Finer Chemical Co., Ltd
  • Indoline pictures
  • Indoline
    496-15-1
  • US $200.00-1.00 / KG
  • 99%, 99.5% Sublimated
  • Henan Fengda Chemical Co., Ltd
  • Indoline pictures
  • Indoline
    496-15-1
  • US $0.00-0.00 / kg
  • 99.0%min
  • Hangzhou ICH Biofarm Co., Ltd
2,3-DIHYDRO-1H-INDOLE HYDROCHLORIDE LABOTEST-BB LT01605668 TIMTEC-BB SBB004291 INDOLINE IDN Indoline.2.3-Dihydroindole 2,3-Dichloro-1H-Indole Indoline,98% Indoline ,97% 1-Azaindan 2,3-Dihydro-1H-indole, 1-Azaindan Indoline, 98% 100GR Indoline, 98% 25GR 1H-Indoline INDOLINE FOR SYNTHESIS 25 ML Two hydrogenindole Indoline ReagentPlus(R), 99% Indoline Vetec(TM) reagent grade, 98% 2,3-dihydro-1h-indol Indoline> Bromfenac Impurity 40 NDOLINE Indoline in stock Factory 2,3-DIHYDRO-1H-INDOLE 1H-Indole, 2,3-dihydro- Dihydroindole 2,3-DIHYDROINDOLE 2-(3-(4-bromobenzoyl)-2-nitrophenyl)acetic acid 496-15-1 Heterocyclic Building Blocks Indoles Indolines Building Blocks AMINE Heterocycle-Indole series Aromatics Heterocycles Intermediates & Fine Chemicals Pharmaceuticals Intermediates Indole/indoline/oxindole Indole and Indoline Indoles and derivatives Pyrroles & Indoles Indoline & Oxindole Pyrroles & Indoles